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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1811012생성일: 2026년 10월 27일

Ethyl orthoformate → 4(3H)-Quinazolinone, 3-(3-bromo-2-methylphenyl)-2-methyl-

https://huagongshe.com/reaction/1811012

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl orthoformateHCID 31214—
반응물AcetanthranilHCID 68236—
반응물3-Bromo-o-toluidineHCID 123538—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물4(3H)-Quinazolinone, 3-(3-bromo-2-methylphenyl)-2-methyl-HCID 6336920%

반응 단계

A solution of 2-methyl-4H-benzo[d][1,3]oxazin-4-one (300 mg, 1.862 mmol), 3-bromo-2-methylaniline (346 mg, 1.862 mmol), and triethoxymethane (276 mg, 1.862 mmol) in THF (2 mL) was heated overnight in a sealed tube at 100° C. The mixture was cooled to rt and diluted with DCM. The solution was washed with water and NaHCO3 (aq), and dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from 90:10 to 50:50 hexane-EtOAc) and the crude product was triturated in hexane to give 3-(3-bromo-2-methylphenyl)-2-methylquinazolin-4(3H)-one as an off-white solid (120 mg, 20%). 1H NMR (400 MHz, chloroform-d) δ 8.28 (1 H, dd, J=7.92, 1.10 Hz), 7.77-7.82 (1 H, m), 7.68-7.73 (2 H, m), 7.47-7.52 (1 H, m), 7.22-7.25 (1 H, m), 7.13-7.17 (1 H, m), 2.20 (6H, s). Mass spectrum m/z 329, 331 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08362065B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-f4b029a191074d4d9cb69579b372c9b5
출처 메모uspto-grants-2013_01